NU-DERM PHYSICAL UV BLOCK

Manufacturer
OMP, Inc. | Swiss-American Products
Effective date
2011-12-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:49:54

Label at a glance#

ProductNU-DERM PHYSICAL UV BLOCK SPF 32
Active ingredientZINC OXIDE
Label structure9 sections

Dosage and administration

Apply liberally to all exposed areas 15 minutes prior to sun exposure and as needed. For children less than 6 months of age, consult a doctor.

Storage and handling

Store at controlled room temperature: 15°-30°C (59°-86°F)

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Zinc oxide 18.5%.

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY. Avoid contact with eyes. If this occurs, rinse with water.

OTC - STOP USE SECTION

OTC - ASK DOCTOR SECTION

Stop use and contact a doctor if rash or irritation develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Apply liberally to all exposed areas 15 minutes prior to sun exposure and as needed. For children less than 6 months of age, consult a doctor.

STORAGE AND HANDLING SECTION

Store at controlled room temperature:
15°-30°C (59°-86°F)

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

bees wax, butylene glycol, cetyl dimethicone, cetyl PEG/PPG-10/1 dimethicone, dimethicone, disodium EDTA, glycereth-26, hydrogenated castor oil, isopropyl palmitate, methylparaben, octyl stearate, propylparaben, purified water, sodium chloride, triethoxycaprylylsilane, tocopherol acetate, willowherb extract

SPL UNCLASSIFIED SECTION

Dist. by OMP Inc. Long Beach, CA 90802

PRINCIPAL DISPLAY PANEL - 57g Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

OBAGI
NU-DERM®

AM
PHYSICAL
UV BLOCK
SPF 32

6

BROAD SPECTRUM UVA/UVB
PHYSICAL SUNBLOCK

18.5% ZINC OXIDE

NET WT. 2 OZ. (57g)

Principal Display Panel
Principal Display Panel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62032-102-362019-11-13C16284748780-197449f38-b5be-f6ea-e053-dbdaa90aa703OBAGI NU-DERM® PHYSICAL UV BLOCK SPF 32

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62032-102NU-DERM PHYSICAL UV BLOCK SPF 32 (ZINC OXIDE) CREAM [OMP, INC.]1Legacy NDC20111230_977d55dd-d775-4ed3-9c11-e48652bb194c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z1
ZINC OXIDEACTIVE MOIETYSOI2LOH54Z1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62032-10262032-102-36

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
af1f08cd-bd8c-4bb2-af97-18507a5e6255977d55dd-d775-4ed3-9c11-e48652bb194c2026-02-11WarningsExact identifier
spl set id: 977d55dd-d775-4ed3-9c11-e48652bb194c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.